Canonical Allele Identifier: CA1216122130

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142088T= , CM000663.2:g.193142088T=	GRCh38
NC_000001.10:g.193111218T= , CM000663.1:g.193111218T=	GRCh37
NC_000001.9:g.191377841T=	NCBI36
NG_012691.1:g.25131T= , LRG_507:g.25131T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+22T= MANE Select	ENSP00000356405.4:n.729+22T=
ENST00000635846.1:c.729+22T=	ENSP00000490035.1:n.729+22T=
ENST00000643006.1:c.729+22T=	ENSP00000496633.1:n.729+22T=
ENST00000643784.1:c.*205+22T=	ENSP00000494944.1:n.*205+22T=
ENST00000647662.1:n.630+22T=
ENST00000648071.1:c.*705+22T=	ENSP00000497513.1:n.*705+22T=
ENST00000649606.1:n.742+22T=
ENST00000649895.1:n.947+22T=
ENST00000650197.1:c.729+22T=	ENSP00000496929.1:n.729+22T=
ENST00000367435.3:c.729+22T=	ENSP00000356405.3:n.729+22T=
NM_024529.4:c.729+22T= , LRG_507t1:c.729+22T=	NP_078805.3:n.729+22T=
XM_006711537.2:c.729+22T=	XP_006711600.1:n.729+22T=
XM_006711537.4:c.729+22T=	XP_006711600.1:n.729+22T=
NM_024529.5:c.729+22T= MANE Select	NP_078805.3:n.729+22T=